未登录Trends in antipsychotic treatment of children and adolescents in Israel from post-mental health reform to post-COVID19 pandemic (2015-2023)以色列儿童和青少年抗精神病药物治疗趋势：从精神卫生改革后到后新冠疫情时期（2015-2023）
Nega, Rachel; Walfisch, Ron; Taler, Michal; Efron, Martin; El Bar, Nurit; Gavze, Revital Perlov; Lev-Shalem, Liat; Bodenheimer, Gilad; Bilu, Yonatan; Gothelf, Doron .png)
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收藏分享 收藏 分享 收藏 分享 收藏 A normative chart for cognitive development in a genetically selected population在遗传选择的人群中认知发展的规范性图表Fiksinski, Ania M.; Bearden, Carrie E.; Bassett, Anne S.; Kahn, Rene S.; Zinkstok, Janneke R.; Hooper, Stephen R.; Tempelaar, Wanda; McDonald-McGinn, Donna; Swillen, Ann; Emanue, Beverly; Morrow, Bernice; Gur, Raquel; Chow, Eva; van den Bree, Marianne; Vermeesch, Joris; Warren, Stephen; Owen, Michael; van Amelsvoor, Therese; Eliez, Stephan; Gothelf, Doron; Celso, Arango; Kates, Wendy; Simon, Tony; Murphy, Kieran; Repetto, Gabriela; Sune, Damian Heine; Vicar, Stefano; Cubells, Joseph; Armando, Marco; Philip, Nicole; Campbell, Linda; Garcia-Minaur, Sixto; Schneider, Maude; Shashi, Vandana; Vorstman, Jacob; Breetvelt, Elemi J. 分享 收藏 A comparative study of the neuropsychiatric and neurocognitive phenotype in two microdeletion syndromes: Velocardiofacial (22q11.2 deletion) and Williams (7q11.23 deletion) syndromes两种微缺失综合征的神经精神和神经认知表型的比较研究: 心面部 (22 q11.2缺失) 和威廉姆斯 (7 q11.23缺失) 综合征Zarchi, O.; Diamond, A.; Weinberger, R.; Abbott, D.; Carmel, M.; Frisch, A.; Michaelovsky, E.; Gruber, R.; Green, T.; Weizman, A.; Gothelf, D. 分享 收藏 Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletionCleynen, Isabelle; Engchuan, Worrawat; Hestand, Matthew S.; Heung, Tracy; Holleman, Aaron M.; Johnston, H. Richard; Monfeuga, Thomas; McDonald-McGinn, Donna M.; Gur, Raquel E.; Morrow, Bernice E.; Swillen, Ann; Vorstman, Jacob A. S.; Bearden, Carrie E.; Chow, Eva W. C.; van den Bree, Marianne; Emanuel, Beverly S.; Vermeesch, Joris R.; Warren, Stephen T.; Owen, Michael J.; Chopra, Pankaj; Cutler, David J.; Duncan, Richard; Kotlar, Alex, V; Mulle, Jennifer G.; Voss, Anna J.; Zwick, Michael E.; Diacou, Alexander; Golden, Aaron; Guo, Tingwei; Lin, Jhih-Rong; Wang, Tao; Zhang, Zhengdong; Zhao, Yingjie; Marshall, Christian; Merico, Daniele; Jin, Andrea; Lilley, Brenna; Salmons, Harold, I; Oanh Tran; Holmans, Peter; Pardinas, Antonio; Walters, James T. R.; Demaerel, Wolfram; Boot, Erik; Butcher, Nancy J.; Costain, Gregory A.; Lowther, Chelsea; Evers, Rens; van Amelsvoort, Therese A. M. J.; van Duin, Esther; Vingerhoets, Claudia; Breckpot, Jeroen; Devriendt, Koen; Vergaelen, Elfi; Vogels, Annick; Crowley, T. Blaine; McGinn, Daniel E.; Moss, Edward M.; Sharkus, Robert J.; Unolt, Marta; Zackai, Elaine H.; Calkins, Monica E.; Gallagher, Robert S.; Gur, Ruben C.; Tang, Sunny X.; Fritsch, Rosemarie; Ornstein, Claudia; Repetto, Gabriela M.; Breetvelt, Elemi; Duijff, Sasja N.; Fiksinski, Ania; Moss, Hayley; Niarchou, Maria; Murphy, Kieran C.; Prasad, Sarah E.; Daly, Eileen M.; Gudbrandsen, Maria; Murphy, Clodagh M.; Murphy, Declan G.; Buzzanca, Antonio; Di Fabio, Fabio; Digilio, Maria C.; Pontillo, Maria; Marino, Bruno; Vicari, Stefano; Coleman, Karlene; Cubells, Joseph F.; Ousley, Opal Y.; Carmel, Miri; Gothelf, Doron; Mekori-Domachevsky, Ehud; Michaelovsky, Elena; Weinberger, Ronnie; Weizman, Abraham; Kushan, Leila; Jalbrzikowski, Maria; Armando, Marco; Eliez, Stephan; Sandini, Corrado; Schneider, Maude; Bena, Frederique Sloan; Antshel, Kevin M.; Fremont, Wanda; Kates, Wendy R.; Belzeaux, Raoul; Busa, Tiffany; Philip, Nicole; Campbell, Linda E.; McCabe, Kathryn L.; Hooper, Stephen R.; Schoch, Kelly; Shashi, Vandana; Simon, Tony J.; Tassone, Flora; Arango, Celso; Fraguas, David; Garcia-Minaur, Sixto; Morey-Canyelles, Jaume; Rosell, Jordi; Suner, Damia H.; Raventos-Simic, Jasna; Epstein, Michael P.; Williams, Nigel M.; Bassett, Anne S. 分享 收藏 Complete Sequence of the 22q11.2 Allele in 1,053 Subjects with 22q11.2 Deletion Syndrome Reveals Modifiers of Conotruncal Heart DefectsZhao, Yingjie; Diacou, Alexander; Johnston, H. Richard; Musfee, Fadi I.; McDonald-McGinn, Donna M.; McGinn, Daniel; Crowley, T. Blaine; Repetto, Gabriela M.; Swillen, Ann; Breckpot, Jeroen; Vermeesch, Joris R.; Kates, Wendy R.; Digilio, M. Cristina; Unolt, Marta; Marino, Bruno; Pontillo, Maria; Armando, Marco; Di Fabio, Fabio; Vicari, Stefano; van den Bree, Marianne; Moss, Hayley; Owen, Michael J.; Murphy, Kieran C.; Murphy, Clodagh M.; Murphy, Declan; Schoch, Kelly; Shashi, Vandana; Tassone, Flora; Simon, Tony J.; Shprintzen, Robert J.; Campbell, Linda; Philip, Nicole; Heine-Suner, Damian; Garcia-Minaur, Sixto; Fernandez, Luis; Bearden, Carrie E.; Vingerhoets, Claudia; van Amelsvoort, Therese; Eliez, Stephan; Schneider, Maude; Vorstman, Jacob A. S.; Gothelf, Doron; Zackai, Elaine; Agopian, A. J.; Gur, Raquel E.; Bassett, Anne S.; Emanuel, Beverly S.; Goldmuntz, Elizabeth; Mitchell, Laura E.; Wang, Tao; Morrow, Bernice E. 分享 收藏 分享 收藏 Deletion size analysis of 1680 22q11.2DS subjects identifies a new recombination hotspot on chromosome 22q11.2Guo, Tingwei; Diacou, Alexander; Nomaru, Hiroko; McDonald-McGinn, Donna M.; Hestand, Matthew; Demaerel, Wolfram; Zhang, Liangtian; Zhao, Yingjie; Ujueta, Francisco; Shan, Jidong; Montagna, Cristina; Zheng, Deyou; Crowley, Terrence B.; Kushan-Wells, Leila; Bearden, Carrie E.; Kates, Wendy R.; Gothelf, Doron; Schneider, Maude; Eliez, Stephan; Breckpot, Jeroen; Swillen, Ann; Vorstman, Jacob; Zackai, Elaine; Benavides Gonzalez, Felipe; Repetto, Gabriela M.; Emanuel, Beverly S.; Bassett, Anne S.; Vermeesch, Joris R.; Marshall, Christian R.; Morrow, Bernice E. 分享 收藏 Rare Genome-Wide Copy Number Variation and Expression of Schizophrenia in 22q11.2 Deletion SyndromeBassett, Anne S.; Lowther, Chelsea; Merico, Daniele; Costain, Gregory; Chow, Eva W. C.; van Amelsvoort, Therese; McDonald-McGinn, Donna; Gur, Raquel E.; Swillen, Ann; Van den Bree, Marianne; Murphy, Kieran; Gothelf, Doron; Bearden, Carrie E.; Eliez, Stephan; Kates, Wendy; Philip, Nicole; Sashi, Vandana; Campbell, Linda; Vorstman, Jacob; Cubells, Joseph; Repetto, Gabriela M.; Simon, Tony; Boot, Erik; Heung, Tracy; Evers, Rens; Vingerhoets, Claudia; van Duin, Esther; Zackai, Elaine; Vergaelen, Elfi; Devriendt, Koen; Vermeesch, Joris R.; Owen, Michael; Murphy, Clodagh; Michaelovosky, Elena; Kushan, Leila; Schneider, Maude; Fremont, Wanda; Busa, Tiffany; Hooper, Stephen; McCabe, Kathryn; Duijff, Sasja; Isaev, Karin; Pellecchia, Giovanna; Wei, John; Gazzellone, Matthew J.; Scherer, Stephen W.; Emanuel, Beverly S.; Guo, Tingwei; Morrow, Bernice E.; Marshall, Christian R. 分享 收藏 Subthreshold Psychosis in 22q11.2 Deletion Syndrome: Multisite Naturalistic StudyWeisman, Omri; Guri, Yael; Gur, Raquel E.; McDonald-McGinn, Donna M.; Calkins, Monica E.; Tang, Sunny X.; Emanuel, Beverly; Zackai, Elaine H.; Eliez, Stephan; Schneider, Maude; Schaer, Marie; Kates, Wendy R.; Antshel, Kevin M.; Fremont, Wanda; Shashi, Vandana; Hooper, Stephen R.; Armando, Marco; Vicari, Stefano; Pontillo, Maria; Kushan, Leila; Jalbrzikowski, Maria; Bearden, Carrie E.; Cubells, Joseph F.; Ousley, Opal Y.; Walker, Elaine F.; Simon, Tony J.; Stoddard, Joel; Niendam, Tara A.; van den Bree, Marianne B. M.; Gothelf, Doron 分享 收藏 分享 收藏 Performance on a computerized neurocognitive battery in 22q11.2 deletion syndrome: A comparison between US and Israeli cohorts22 q11.2缺失综合征中计算机神经认知电池的性能: 美国和以色列队列之间的比较Yi, James J.; Weinberger, Ronnie; Moore, Tyler M.; Calkins, Monica E.; Guri, Yael; McDonald-McGinn, Donna M.; Zackai, Elaine H.; Emanuel, Beverly S.; Gur, Raquel E.; Gothelf, Doron; Gur, Ruben C. 分享 收藏 Rare copy number variants and congenital heart defects in the 22q11.2 deletion syndromeMlynarski, Elisabeth E.; Xie, Michael; Taylor, Deanne; Sheridan, Molly B.; Guo, Tingwei; Racedo, Silvia E.; McDonald-McGinn, Donna M.; Chow, Eva W. C.; Vorstman, Jacob; Swillen, Ann; Devriendt, Koen; Breckpot, Jeroen; Digilio, Maria Cristina; Marino, Bruno; Dallapiccola, Bruno; Philip, Nicole; Simon, Tony J.; Roberts, Amy E.; Piotrowicz, Malgorzata; Bearden, Carrie E.; Eliez, Stephan; Gothelf, Doron; Coleman, Karlene; Kates, Wendy R.; Devoto, Marcella; Zackai, Elaine; Heine-Suner, Damian; Goldmuntz, Elizabeth; Bassett, Anne S.; Morrow, Bernice E.; Emanuel, Beverly S. 分享 收藏 Copy-Number Variation of the Glucose Transporter Gene SLC2A3 and Congenital Heart Defects in the 22q11.2 Deletion SyndromeMlynarski, Elisabeth E.; Sheridan, Molly B.; Xie, Michael; Guo, Tingwei; Racedo, Silvia E.; McDonald-McGinn, Donna M.; Gai, Xiaowu; Chow, Eva W. C.; Vorstman, Jacob; Swillen, Ann; Devriendt, Koen; Breckpot, Jeroen; Digilio, Maria Cristina; Marino, Bruno; Dallapiccola, Bruno; Philip, Nicole; Simon, Tony J.; Roberts, Amy E.; Piotrowicz, Malgorzata; Bearden, Carrie E.; Eliez, Stephan; Gothelf, Doron; Coleman, Karlene; Kates, Wendy R.; Devoto, Marcella; Zackai, Elaine; Heine-Suner, Damian; Shaikh, Tamim H.; Bassett, Anne S.; Goldmuntz, Elizabeth; Morrow, Bernice E.; Emanuel, Beverly S. 分享 收藏 分享 收藏 Thymic and bone marrow output in individuals with 22q11.2 deletion syndromeDar, Nina; Gothelf, Doron; Korn, David; Frisch, Amos; Weizman, Abraham; Michaelovsky, Elena; Carmel, Miri; Yeshayahu, Yonatan; Dubnov-Raz, Gal; Pessach, Itai M.; Simon, Amos J.; Lev, Atar; Somech, Raz 分享 收藏 分享 收藏 Psychiatric Disorders From Childhood to Adulthood in 22q11.2 Deletion Syndrome: Results From the International Consortium on Brain and Behavior in 22q11.2 Deletion SyndromeSchneider, Maude; Debbane, Martin; Bassett, Anne S.; Chow, Eva W. C.; Fung, Wai Lun Alan; van den Bree, Marianne B. M.; Owen, Michael; Murphy, Kieran C.; Niarchou, Maria; Kates, Wendy R.; Antshel, Kevin M.; Fremont, Wanda; McDonald-McGinn, Donna M.; Gur, Raquel E.; Zackai, Elaine H.; Vorstman, Jacob; Duijff, Sasja N.; Klaassen, Petra W. J.; Swillen, Ann; Gothelf, Doron; Green, Tamar; Weizman, Abraham; Van Amelsvoort, Therese; Evers, Laurens; Boot, Erik; Shashi, Vandana; Hooper, Stephen R.; Bearden, Carrie E.; Jalbrzikowski, Maria; Armando, Marco; Vicari, Stefano; Murphy, Declan G.; Ousley, Opal; Campbell, Linda E.; Simon, Tony J.; Eliez, Stephan 分享 收藏 
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